Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Diethylamine | HCID 8021 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 2,3-Dihydro-1,4-benzodioxin-5-carboxylic acid | HCID 78184 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 70149605 | HCID 70149605 | 96% |
Reaction Steps
Into a 250 ml round bottom flask fitted with a nitrogen inlet and magnetic stirring bar were placed 32.8 ml of benzene and 2,3-ethylenedioxybenzoic acid (2.96 g, 16.4 mmol). The mixture was stirred into a suspension before adding oxalyl chloride (4.3 ml, 8.88 mmol) via a syringe. The mixture was cooled to 0° and 5 drops of dimethylformamide added. The mixture was allowed to warm to room temperature over 1 hour before concentrating the mixture in vacuo. The residue was taken up in 52.5 ml of anhydrous tetrahydrofuran and cooled to 0° before adding diethylamine (17 ml, 164 mmol) dropwise over 10 minutes. The mixture was then allowed to warm to room temperature and diluted with ethyl acetate. The mixture was washed twice with brine, dried over sodium sulfate, filtered, and concentrated to give 3.71 g of subtitled product (96%) which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06376505B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-f14480480eba4a8e94f42a446ab92795 |
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| Source note | uspto-grants-2002_04 |
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